JPH03123711A - Miticide composition - Google Patents

Miticide composition

Info

Publication number
JPH03123711A
JPH03123711A JP1262710A JP26271089A JPH03123711A JP H03123711 A JPH03123711 A JP H03123711A JP 1262710 A JP1262710 A JP 1262710A JP 26271089 A JP26271089 A JP 26271089A JP H03123711 A JPH03123711 A JP H03123711A
Authority
JP
Japan
Prior art keywords
mites
alpha
parts
fenpropathrin
cyano
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP1262710A
Other languages
Japanese (ja)
Other versions
JP2813993B2 (en
Inventor
Terukazu Morimoto
森本 輝一
Haruo Sasayama
笹山 晴男
Noriyoshi Kasamatsu
笠松 紀美
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TOMONO NOYAKU KK
Sumitomo Chemical Co Ltd
Original Assignee
TOMONO NOYAKU KK
Sumitomo Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by TOMONO NOYAKU KK, Sumitomo Chemical Co Ltd filed Critical TOMONO NOYAKU KK
Priority to JP1262710A priority Critical patent/JP2813993B2/en
Priority to US07/589,598 priority patent/US5120721A/en
Priority to IT04834190A priority patent/IT1247726B/en
Priority to ES9002527A priority patent/ES2032255B1/en
Priority to KR1019900015789A priority patent/KR0168434B1/en
Priority to FR909012283A priority patent/FR2652716B1/en
Priority to CN90108223A priority patent/CN1033356C/en
Publication of JPH03123711A publication Critical patent/JPH03123711A/en
Application granted granted Critical
Publication of JP2813993B2 publication Critical patent/JP2813993B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/12Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain a miticide composition effectively controllable drug-resistant mites living within agricultural and horticultural crops without chemical injury to crops by jointly using fenpropathrin or fluvalinate and ethion with synergistically enhancing mite-killing effect of individual component. CONSTITUTION:A miticide composition quickly affecting and continuously exhibiting synergistic control effect on said mites such as two-spotted spider mites is obtained by containing (A) alpha-cyano-3phenoxybenzyl 2,2,3,3-tetramethyl cyclopropane carboxylate (fenpropathrin) or alpha-cyano-3-phenoxybenzyl N-(2- chloro-alpha,alpha,alpha-trifluoro-p-tolyl) valinate (fluvalinate), especially the former and (B) O,O,O,O-tetraethyl S,S-methylene bisphosphorodithioate (ethion) as active ingredients, in a weight ratio of A:B=1:(1-100) and A+B=1-80wt.% of whole drug.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明はハダニ類を始めサビダニ類、ホコリダニ類等の
ダニ類を有効に防除することの出来る新規な殺ダニ剤組
成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a novel acaricide composition that can effectively control mites such as spider mites, rust mites, and dust mites.

〈従来の技術〉 有機リン殺虫剤の中には殺ダニ活性を有するものもいく
つかあるが、有機リン剤抵抗性ハダニ類の蔓延などによ
り、現在では殺ダニ剤として十分な効果を発揮するもの
は少ない。合成ピレスロイド剤においても、殺ダニ活性
の最も高いグループでもハダニ類に対する防除効果は十
分ではない。
<Prior art> Some organophosphorus insecticides have acaricidal activity, but due to the spread of organophosphate-resistant spider mites, it is currently difficult to find any that are sufficiently effective as acaricides. There are few. Among synthetic pyrethroids, even the group with the highest acaricidal activity does not have sufficient control effects against spider mites.

以上の欠点を補うため、有機リン殺虫剤と合成ピレスロ
イド剤を混合した殺ダニ剤組成物として、既に1、フエ
ンプロバトリンとアセフェートを混合した剤(特開昭6
3−145206号公報)、フェンプロパトリンとジメ
トエートなどを混合した剤(特開昭56−29509号
公報)、ニチオンとジベルメトリンなどとを混合した剤
(特開昭58−128309号公報)などが知られてい
るが、効力などの点で必ずしも十分であるとは言えない
In order to compensate for the above-mentioned drawbacks, an acaricide composition containing an organic phosphorus insecticide and a synthetic pyrethroid has already been developed.
3-145206), a mixture of fenpropathrin and dimethoate (Japanese Unexamined Patent Publication No. 56-29509), and a mixture of nithion and dibermethrin (Japanese Unexamined Patent Publication No. 128309-1982). However, it cannot be said that it is necessarily sufficient in terms of effectiveness.

その他、ジコホル、酸化フェンブタスズ、ヘキシチアゾ
クス等の殺ダニ専用剤も知られているが、近年、これら
殺ダニ専用剤の効果も低下し、新しい殺ダニ剤の開発が
望まれている。
In addition, miticide-specific agents such as dicofol, fenbutastin oxide, and hexythiazox are also known, but in recent years, the effectiveness of these miticide-specific agents has decreased, and the development of new miticides has been desired.

〈発明が解決しようとする課題〉 多くの殺ダニ剤が長年にわたって使用された結果、これ
らの殺ダニ剤に対して強い抵抗性を示すダニ類が各地に
出現してきた。そのなかでも、果樹、野菜、茶、花木な
どに寄生するナミハダニ、ニセナミハダニ、カンザワハ
ダニ、ミカンハダニ、リンゴハダニ、チャノホコリダニ
などは特に薬剤抵抗性の発達が著しい。そのためこれら
のダニ類に対しては、多くの殺ダニ剤が実用性を失いつ
、つある。
<Problems to be Solved by the Invention> As a result of many acaricides being used for many years, mites that exhibit strong resistance to these acaricides have appeared in various places. Among them, drug-resistant spider mites, such as the two-spotted spider mite, false two-spotted spider mite, Kanzawa spider mite, citrus spider mite, apple spider mite, and teal dust mite, which parasitize fruit trees, vegetables, tea, flowering trees, etc., have developed remarkable drug resistance. Therefore, many acaricides have lost their practical use against these mites.

したがって、従来の殺ダニ剤の使用により抵抗性が発達
したダニ類に対しても低薬量で効果が高く、しかも毒性
面や環境への悪影響も少ない新規な殺ダニ剤の開発が強
く望まれている。
Therefore, there is a strong desire to develop new acaricides that are highly effective at low doses even against mites that have developed resistance due to the use of conventional acaricides, and that have less toxicity and less negative impact on the environment. ing.

本発明の目的はこのような要望に合致した新規な殺ダニ
剤を提供することにある。
An object of the present invention is to provide a new acaricide that meets these needs.

く課題を解決するための手段〉 本発明者らは、このような現状に対処するため、鋭意検
討を重ね、以下に示す組成物が顕著な効果を示すことを
見いだし、本発明を完成した。すなわち本発明は、活性
成分として(a)α−シアノ−3−フェノキシベンジル
2.2,3.3−テトラメチルシクロプロパンカルボキ
シレート(以下、「フェンプロパトリン」という)また
はα−シアノ−3−フェノキシベンジル N−(2−ク
ロロ−α、α、α−トリフルオロ−p−)リル)バリネ
ート(以下、「フルパリネート」という) と、 (b)O,0,0,0−テトラエチル S。
Means for Solving the Problems> In order to cope with the current situation, the present inventors have made extensive studies and have found that the composition shown below exhibits remarkable effects, and have completed the present invention. That is, the present invention provides (a) α-cyano-3-phenoxybenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate (hereinafter referred to as "fenpropathrin") or α-cyano-3-phenoxybenzyl as an active ingredient. Phenoxybenzyl N-(2-chloro-α,α,α-trifluoro-p-)lyl)valinate (hereinafter referred to as “fluparinate”) and (b) O,0,0,0-tetraethyl S.

S−メチレン ビスフォスフォロジチオエート(以下、
「ニチオン」という) とを含有することを特徴とする殺ダニ剤組成物(以下、
本発明組成物と称す)を提供するものである。
S-methylene bisphosphorodithioate (hereinafter referred to as
An acaricide composition (hereinafter referred to as "Nithion") characterized by containing the following:
composition of the present invention).

本発明組成物は、フエンプロバトリンまたはフルパリネ
ートとニチオンを併用することにより、果樹、野菜、茶
、花木などのナミハダニ、ニセナミハダニ、カンザワハ
ダニ、ミカンハダニ、リンゴハダニ、チャノホコリダニ
などのダニ類に対して単独使用には見られない優れた殺
ダニ効果を発揮するようになる。すなわち、1、 農園
芸作物に寄生するナミハダニ、ミカンハダニ、カンザワ
ハダニなどのダニ類に対して、各々の活性成分の単独使
用に比べて相乗的な防除効果が発揮される。しかもその
効果は速効的に現れるとともに、その効果が持続して、
高い相乗的殺ダニ効果が発現される。その結果、単独使
用では金(無効となってしまう場合でも、併用によりこ
れらのダニ類を速効的かつ長期にわたって完全に防除す
ることができるようになる。
By using fuenprobatrin or fluparinate in combination with Nithion, the composition of the present invention can be used alone against mites such as two-spotted spider mites, false two-spotted spider mites, Kanzawa spider mites, citrus spider mites, apple spider mites, and teal dust mites on fruit trees, vegetables, tea, flowering trees, etc. It now exhibits an excellent acaricidal effect that is not seen in other plants. That is, 1. A synergistic control effect is exhibited against mites such as two-spotted spider mite, citrus spider mite, and Kanzawa spider mite that parasitize agricultural and horticultural crops, compared to the use of each active ingredient alone. Moreover, the effect appears quickly, and the effect lasts for a long time.
A high synergistic acaricidal effect is expressed. As a result, even if gold is ineffective when used alone, when used in combination, these mites can be completely controlled quickly and over a long period of time.

2、 多(の有機合成殺ダニ剤により抵抗性が発達した
ダニ類に対しても、顕著な殺ダニ効果を発揮する。
2. It exhibits a remarkable acaricidal effect even against mites that have developed resistance to organic synthetic acaricides.

3、 農園芸作物に対して問題となる薬害などを与える
こともない。
3. It does not cause harmful chemical damage to agricultural and horticultural crops.

4、 本発明組成物は、既に殺ダニ剤組成物として出願
されているフェンプロパトリンとアセフェートを混合し
た剤(特開昭63−145206号公報)、フエンプロ
パトリンとジメトエートなどを混合した剤(特開昭56
−29509号公報)およびニチオンとジベルメトリン
などとを混合した剤(特開昭58−128309号公報
)に比較しても明らかに優れた殺ダニ活性を有する。
4. The composition of the present invention is a mixture of fenpropathrin and acephate (Japanese Unexamined Patent Publication No. 145206/1983), which has already been applied as an acaricide composition, and a mixture of fenpropathrin and dimethoate ( Japanese Unexamined Patent Publication 1983
-29509) and a mixture of nithion and dibermethrin (Japanese Unexamined Patent Publication No. 128309/1982), it has clearly superior acaricidal activity.

本発明組成物は、特にダニ類の成虫、幼若虫に対して速
効的に作用し、しかも効果の持続性にも優れてシする。
The composition of the present invention is particularly effective against adults and nymphs of mites, and has excellent long-lasting effects.

さらに、他の害虫に対して各々の成分が本来有する優れ
た殺虫活性は、混用により何ら損なわれることはない。
Furthermore, the excellent insecticidal activity of each component against other pests is not impaired in any way by mixed use.

以下本発明組成物の製剤化方法および使用方法について
具体的に説明する。
The method for formulating and using the composition of the present invention will be specifically explained below.

本発明組成物を製造するには、本発明の活性成分と適当
な担体および補助剤、たとえば界面活性剤、結合剤、安
定剤などを配合し、常法によって水和剤、乳剤、フロア
ブル剤、粉剤、DL(ドリフトレス型)粉剤などに製剤
化すればよい。
In order to produce the composition of the present invention, the active ingredient of the present invention is blended with suitable carriers and auxiliary agents such as surfactants, binders, stabilizers, etc., and the compositions are prepared as wettable powders, emulsions, flowables, etc. by conventional methods. It may be formulated into a powder, DL (driftless type) powder, or the like.

この場合、フェンブロパトリンまたはフルパリネートと
ニチオンとの混合比は1対1〜1対100、好ましくは
1対1〜1対50であり、製剤中の活性成分含有量合計
(重量比)は1〜80%である。
In this case, the mixing ratio of fenbropatrine or fluparinate and nithion is 1:1 to 1:100, preferably 1:1 to 1:50, and the total active ingredient content (weight ratio) in the preparation is 1 to 1:1. It is 80%.

本発明組成物において使用できる担体としては、農園芸
用薬剤に常用されるものであれば固体または液体のいず
れでも使用でき、特定のものに限定されるものではない
As the carrier that can be used in the composition of the present invention, any solid or liquid carrier commonly used for agricultural and horticultural chemicals can be used, and the carrier is not limited to a specific carrier.

たとえば、固体担体としては、鉱物質粉末、植物質粉末
、アルミナ、珪酸塩、糖重合体、ワックスなどが挙げら
れる。
For example, solid carriers include mineral powders, vegetable powders, alumina, silicates, sugar polymers, waxes, and the like.

また、液体担体としては、水、アルコール類、芳香族炭
化水素類、ハロゲン化炭化水素類、エーテル類、ケトン
類、エステル類、ニトリル類、アルコールエーテル類、
脂肪族または脂環式炭化水素類、工業用ガソリンおよび
石油留分などが挙げられる。
In addition, liquid carriers include water, alcohols, aromatic hydrocarbons, halogenated hydrocarbons, ethers, ketones, esters, nitriles, alcohol ethers,
Examples include aliphatic or cycloaliphatic hydrocarbons, industrial gasoline and petroleum fractions.

また、乳剤、水和剤、フロアブル剤などの製剤化に際し
ては、乳化、分散、可溶化、湿潤、発泡、潤滑、拡展な
どの目的で界面活性剤または乳化剤などが使用される。
Furthermore, when formulating emulsions, wettable powders, flowable preparations, etc., surfactants or emulsifiers are used for purposes such as emulsification, dispersion, solubilization, wetting, foaming, lubrication, and spreading.

さらに必要に応じて、酸化防止剤、紫外線吸収剤などの
ような安定化剤を適量加えることもできる。
Further, if necessary, a suitable amount of stabilizers such as antioxidants and ultraviolet absorbers can be added.

また、本発明組成物は、他の殺ダニ剤、殺虫剤、誘引剤
、忌避剤、殺菌剤、植物生長調節剤、肥料などと混合し
て用いることができ、かかる混用により適用性(適用病
害虫、使用方法、使用時期など)の拡大をはかることが
できる。
Furthermore, the composition of the present invention can be mixed with other acaricides, insecticides, attractants, repellents, fungicides, plant growth regulators, fertilizers, etc. , how to use it, when to use it, etc.).

本発明組成物の使用方法は次のとおりである。The method of using the composition of the present invention is as follows.

すなわち、施用量は作物の大きさにより異なるが、一般
にlOアール当り活性成分型でフェンプロパトリンまた
はフルパリネートとニチオンの合計量が0.3〜550
gであり、好ましくは2〜150gである。これを散布
するには水和剤または乳剤では水で希釈し、ダニ類の発
生する時期に作物に通常10アール当り30〜2000
1、好ましくは50〜5001の適用量で処理する。
That is, the application rate varies depending on the size of the crop, but generally the total amount of fenpropathrin or fluparinate and nithione in the active ingredient form is 0.3 to 550 per 10 are.
g, preferably 2 to 150 g. To spray this, dilute it with water for wettable powders or emulsions, and spray it on crops during the mite outbreak season, usually at a rate of 30 to 2,000 per 10 ares.
1, preferably at an application rate of 50 to 5001.

本発明組成物は、カンキツ類ではミカンハダニ、ミカン
サビダニ、落葉果樹類ではリンゴハダニ、ナミハダニ、
オウトウハダニ、カンザワハダニ、ニセナミハダニ、茶
ではカンザワハダニ、野菜、花木ではナミハダニ、カン
ザワハダニ、ニセナミハダニ、チャノホコリダニ等のダ
ニ類に対して、各々の活性成分の単独施用に比べて相乗
的に防除効果が発揮され、これらのダニ類を極めて効果
的に防除することができる。
The composition of the present invention can be applied to citrus fruits such as citrus spider mites, citrus rust mites, and deciduous fruit trees such as apple spider mites and two-spotted spider mites.
It exhibits a synergistic control effect against mites such as the Japanese red spider mite, Kanzawa spider mite, false red spider mite, Kanzawa spider mite for tea, and the white spider mite, Kanzawa spider mite, false red spider mite, false red spider mite, and tea dust mite for tea, vegetables, and flowering plants compared to the individual application of each active ingredient. , these mites can be controlled extremely effectively.

本発明組成物の活性成分であるフエンプロパトリン、フ
ルパリネートおよびニチオンの化学構造式を第1表に示
す。
Table 1 shows the chemical structural formulas of fenpropathrin, fluparinate and nithione, which are the active ingredients of the composition of the present invention.

第1表 これらのうち、フエンプロパトリンおよびフルパリネー
トには立体異性体が存在するが、本発明にはそれらのう
ち、殺ダニ活性上有効な異性体およびそれらの混合物も
含まれる。
Table 1 Among these, fenpropathrin and fluparinate have stereoisomers, and the present invention also includes isomers effective in acaricidal activity and mixtures thereof.

〈実施例〉 以下に若干の実施例を挙げるが、活性成分の配合割合、
補助成分およびその添加量などは以下の実施例のみに限
定されるものではない。なお、実施例において部とある
のはすべて重量部を表わす。
<Examples> Some examples are listed below, but the blending ratio of active ingredients,
The auxiliary components and the amounts added thereof are not limited to the following examples. In addition, all parts in the examples represent parts by weight.

実施例1 フエンブロパトリンまたはフルパリネート10部、ニチ
オン30部、ラウリル硫酸ナトリウム塩5部、ナフタレ
ンスルホン酸ソーダホルマリン縮合物2部、ホワイトカ
ーボン20部、クレー33部を均一に混合粉砕して水和
剤を得る。
Example 1 10 parts of fenbropathrin or fluparinate, 30 parts of nithion, 5 parts of sodium lauryl sulfate, 2 parts of naphthalene sulfonic acid sodium formalin condensate, 20 parts of white carbon, and 33 parts of clay were uniformly mixed and ground to form a wettable powder. get.

実施例2 フエンプロバトリンまたはフルパリネート10部、ニチ
オン10部、ツルポール2564(東邦化学製、非イオ
ン、陰イオン混合配合乳化剤)15部、キジロール65
部を混合溶解して乳剤を得る。
Example 2 10 parts of fenprobatrin or fluparinate, 10 parts of Nithion, 15 parts of Tsurpol 2564 (manufactured by Toho Chemical, nonionic and anionic mixed emulsifier), 65 parts of Kijirol
An emulsion is obtained by mixing and dissolving the two parts.

実施例3 フェンブロバトリンまたはフルパリネート5部、ニチオ
ン35部、ツルポール2564 (東邦化学製、非イオ
ン、陰イオン混合配合乳化剤)15部、キジロール45
部を混合溶解して乳剤を得る。
Example 3 5 parts of fenbrobatrin or fluparinate, 35 parts of Nithion, 15 parts of Tsurpol 2564 (manufactured by Toho Chemical, nonionic and anionic mixed emulsifier), 45 parts of Kijirol
An emulsion is obtained by mixing and dissolving the two parts.

実施例4 フエンプロパトリンまたはフルパリネート5部、ニチオ
ン30部、ラウリル硫酸ナトリウム塩5部、ナフタレン
スルホン酸ソーダホルマリン縮合物2部、ホワイトカー
ボン20部、クレー38部を均一に混合粉砕して水和剤
を得る。
Example 4 5 parts of fenpropathrin or fluparinate, 30 parts of nithion, 5 parts of sodium lauryl sulfate, 2 parts of naphthalene sulfonic acid sodium formalin condensate, 20 parts of white carbon, and 38 parts of clay were uniformly mixed and ground to make a wettable powder. get.

次に本発明組成物の作用効果と有用性を試験例を挙げて
説明する。
Next, the effects and usefulness of the composition of the present invention will be explained by giving test examples.

試験例1 ガラス温室内に植えた夏みかん実生で累代飼育中の有機
リン剤や有機スズ剤およびヘキンチアゾクスに抵抗性を
示すミカンハダニ雌成虫および卵に対する殺ダニ活性を
室内試験で検討した。すなわち、寒天ゲル上に固定した
みかん葉にミカンハダニ雌成虫を接種し、1日間産卵さ
せた後、定量散布装置により、実施例2および実施例3
に準じて調整した本発明の乳剤の所定濃度水希釈液を1
0アール当り30j7相当量ずつ散布し、2日後に殺成
虫効果、10日後に殺卵効果を調べた。本試験は1薬液
処理につき成虫lO個体2区制で行なった。その結果は
第2表のとおりである。なお以下の試験例において殺卵
効果とは、殺卵および殺ふ化幼虫を合わせ−6゜ 試験例2 25℃恒温条件の室内でインゲンの幼苗により累代飼育
中の有機リン剤や有機スズ剤に抵抗性を示すカンザワハ
ダニ雌成虫および卵に対する殺ダニ活性を室内試験で検
討した。すなわち、寒天ゲル上に固定したインゲン葉に
カンザワハダニ雌成虫を接種し、1日間産卵させた後、
定量散布装置により、本発明の組合せを含む合成ピレス
ロイド剤と有機リン剤の単用および混用の所定濃度水希
釈液をlOアール当り3(l相当量ずつ散布し、2日後
に殺成虫効果、9日後に殺卵効果を調べた。本試験はl
薬液処理につき成虫lO個体2区制で行なった。その結
果は第3表のとおりである。
Test Example 1 The acaricidal activity against adult female citrus spider mites and eggs, which are resistant to organic phosphorus agents, organic tin agents, and hechinthiazox, and which are resistant to organic phosphorus agents, organic tin agents, and hechinthiazox, was investigated in a laboratory test using summer tangerine seedlings planted in a glass greenhouse. That is, female adult citrus spider mites were inoculated onto tangerine leaves fixed on agar gel, and after spawning for one day, Example 2 and Example 3 were sprayed using a quantitative spraying device.
A predetermined concentration water dilution solution of the emulsion of the present invention prepared according to
It was sprayed in an amount equivalent to 30j7 per area, and the adulticidal effect was examined after 2 days and the ovicidal effect after 10 days. This test was conducted in two groups with 10 adult insects per chemical solution treatment. The results are shown in Table 2. In the following test examples, the ovicidal effect refers to the combination of ovicidal and hatchicidal larvae. The acaricidal activity against adult female Kanzawa spider mites and their eggs was investigated in a laboratory test. Specifically, female Kanzawa spider mites were inoculated onto kidney bean leaves fixed on agar gel, and after allowing them to lay eggs for one day,
Using a quantitative spraying device, a predetermined concentration water diluted solution of single or mixed synthetic pyrethroids and organic phosphorus agents containing the combination of the present invention is sprayed in an amount equivalent to 3 (liter) per 10 are, and after 2 days, the adulticidal effect is 9. The ovicidal effect was examined after 1 day.
The chemical treatment was carried out in two groups with 10 adult insects. The results are shown in Table 3.

試験例3 ガラス温室内に植えた5〜6葉期インゲンに累代飼育中
の有機リン剤や有機スズ剤に抵抗性を示すナミハダニ雌
成虫を1株当り20個体ずつ接種して定着産卵させた。
Test Example 3 Twenty female adult two-spotted spider mites, which are resistant to organic phosphorus agents and organic tin agents, which are resistant to organic phosphorus agents and organic tin agents during continuous rearing, were inoculated into 5- to 6-leaf stage green beans planted in a glass greenhouse, and settled and laid eggs.

そして、定着、産卵7日後に実施例1に準じて調整した
本発明の水和剤の所定濃度水希釈液を手押し式噴霧器に
て10アール当り100j7相当量ずつ散布した。
Seven days after establishment and spawning, a predetermined concentration diluted water solution of the hydrating agent of the present invention prepared according to Example 1 was sprayed using a hand sprayer in an amount equivalent to 100j7 per 10 are.

散布直前、散布3日後、10日後、20日後、30日後
に、寄生しているハダニ雌成虫数および薬害を調べ、防
除価(%)を算出した。
Immediately before spraying, 3 days, 10 days, 20 days, and 30 days after spraying, the number of parasitic female adult spider mites and chemical damage were determined, and the control value (%) was calculated.

本試験は1薬液処理につき1株、3区制で行なった。そ
の結果は第4表のとおりである。なお、試験例中の防除
価(%)は次式により算出Ca:無散布区散布前虫数 Cb=無散布区散布後虫数 Ta:散布区散布前虫数 Tb:散布区散布後虫数 試験例4 ミカンハダニが多発生している10号素焼鉢植え興津早
生温州みかんを用いて実施例3に準じて調整した本発明
の乳剤の所定濃度水希釈液を手押し式噴霧器にて10ア
ール当り3001相当量ずつ散布した。散布直前、散布
3日後、10日後、20日後、30日後に、1樹当り任
意の20葉につき寄生しているハダニ雌成虫数および薬
害を調べ、防除価(%)を算出した。
This test was conducted in three plots, with one plant per chemical solution treatment. The results are shown in Table 4. In addition, the control value (%) in the test example is calculated using the following formula: Ca: Number of insects in non-sprayed area before spraying Cb = Number of insects in non-sprayed area after spraying Ta: Number of insects in sprayed area before spraying Tb: Number of insects in sprayed area after spraying Test Example 4 A predetermined concentration water dilution of the emulsion of the present invention prepared according to Example 3 was applied using a hand-held sprayer using a No. 10 unglazed potted Okitsu-Wase Satsuma mandarin orange in which mandarin orange spider mites are frequently found. It was distributed in small amounts. Immediately before spraying, 3 days after spraying, 10 days after, 20 days after, and 30 days after spraying, the number of parasitic female adult spider mites and chemical damage on arbitrary 20 leaves per tree were examined, and the control value (%) was calculated.

本試験は1薬液処理につき1樹、3区制で行なった。そ
の結果は第5表のとおりである。
This test was conducted in three plots with one tree per chemical treatment. The results are shown in Table 5.

試験例5 累代飼育中の、有機リン剤に抵抗性を示すナミハダニ雌
成虫を、人工気象室内でポット(直径9an)植えイン
ゲンに寄生させた。そのインゲンに実施例4に準じて調
製した本発明の水和剤の所定濃度水希釈液を3ポツトあ
たり3〇−散布した。ポットは25℃±1°Cの室内に
て保管した。散布前及び散布後の所定臼にナミ/’tダ
ニ雌成虫数を調査した。その結果は第6表のと7 〈発明の効果〉
Test Example 5 Adult female two-spotted spider mites, which had been reared for generations and were resistant to organic phosphorus agents, were parasitized on green beans planted in pots (diameter 9an) in an artificial climate room. A predetermined concentration water dilution solution of the hydrating agent of the present invention prepared according to Example 4 was sprayed on the green beans at 30 kg per 3 pots. The pots were stored indoors at 25°C ± 1°C. The number of female adult Nami/'t mites was investigated on designated mortars before and after spraying. The results are shown in Table 6 and 7. <Effects of the invention>

Claims (2)

【特許請求の範囲】[Claims] (1)(a)α−シアノ−3−フェノキシベンジル2,
2,3,3−テトラメチルシクロプロパンカルボキシレ
ートまたはα−シアノ−3−フェノキシベンジルN−(
2−クロロ−α,α,α−トリフルオロ−p−トリル)
バリネートと、 (b)O,O,O,O−テトラエチルS, S−メチレンビスフォスフォロジチオエーとを活性成分
として含有することを特徴とする殺ダニ剤組成物。
(1) (a) α-cyano-3-phenoxybenzyl 2,
2,3,3-tetramethylcyclopropanecarboxylate or α-cyano-3-phenoxybenzyl N-(
2-chloro-α,α,α-trifluoro-p-tolyl)
A miticide composition comprising valinate and (b) O,O,O,O-tetraethyl S,S-methylenebisphosphorodithioate as active ingredients.
(2)α−シアノ−3−フェノキシベンジル2,2,3
,3−テトラメチルシクロプロパンカルボキシレートと
O,O,O,O−テトラエチルS,S−メチレンビスフ
ォスフォロジチオエートとを活性成分として含有するこ
とを特徴とする殺ダニ剤組成物。
(2) α-cyano-3-phenoxybenzyl 2,2,3
, 3-tetramethylcyclopropanecarboxylate and O,O,O,O-tetraethyl S,S-methylenebisphosphorodithioate as active ingredients.
JP1262710A 1989-10-06 1989-10-06 Acaricide composition Expired - Lifetime JP2813993B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP1262710A JP2813993B2 (en) 1989-10-06 1989-10-06 Acaricide composition
US07/589,598 US5120721A (en) 1989-10-06 1990-09-28 Acaricidal composition
IT04834190A IT1247726B (en) 1989-10-06 1990-10-04 ACARICIDE COMPOSITION AND PROCEDURE FOR ITS PRODUCTION.
KR1019900015789A KR0168434B1 (en) 1989-10-06 1990-10-05 Acaricidal composition
ES9002527A ES2032255B1 (en) 1989-10-06 1990-10-05 ACARICIDAL COMPOSITION.
FR909012283A FR2652716B1 (en) 1989-10-06 1990-10-05 ACARICIDAL COMPOSITION BASED ON ETHION AND FENPROPATHRIN OR FLUVALINATE.
CN90108223A CN1033356C (en) 1989-10-06 1990-10-05 Acaricidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1262710A JP2813993B2 (en) 1989-10-06 1989-10-06 Acaricide composition

Publications (2)

Publication Number Publication Date
JPH03123711A true JPH03123711A (en) 1991-05-27
JP2813993B2 JP2813993B2 (en) 1998-10-22

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JP1262710A Expired - Lifetime JP2813993B2 (en) 1989-10-06 1989-10-06 Acaricide composition

Country Status (7)

Country Link
US (1) US5120721A (en)
JP (1) JP2813993B2 (en)
KR (1) KR0168434B1 (en)
CN (1) CN1033356C (en)
ES (1) ES2032255B1 (en)
FR (1) FR2652716B1 (en)
IT (1) IT1247726B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3163461B2 (en) * 1992-10-19 2001-05-08 大塚化学株式会社 Insecticide, acaricide composition
ZA952100B (en) * 1994-03-16 1995-12-11 Sankyo Co Pesticidal combinations
CN101503855B (en) * 2008-02-04 2012-04-18 上海德桑精细化工有限公司 Antibacterial anti-mite finishing agent for fabric
US9168288B2 (en) 2010-04-09 2015-10-27 Mount Sinai Hospital Methods for treating disorders of the gastrointestinal tract using a GLP-1 agonist

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2873228A (en) * 1956-07-16 1959-02-10 Fmc Corp Pesticidal phosphorus esters
JPS515450B1 (en) * 1971-06-29 1976-02-20
US4243819A (en) * 1978-02-16 1981-01-06 Zoecon Corporation Substituted amino acids
JPS5629509A (en) * 1979-08-20 1981-03-24 Sumitomo Chem Co Ltd Acaricidal composition
GB2063672B (en) * 1979-11-14 1983-04-07 Shell Int Research Pesticidal compositions
US4260633A (en) * 1980-04-21 1981-04-07 Zoecon Corporation Pesticidal esters of amino acids
FR2520197A1 (en) * 1982-01-25 1983-07-29 Rhone Poulenc Agrochimie ETHION AND PYRETHROID-BASED INSECTICIDE AND ACARICIDE COMPOSITIONS AND PROCESS FOR TREATING ARTHROPODIC VEGETABLES USING THE SAME
FR2581509B1 (en) * 1985-05-07 1988-09-09 Sandoz Sa Produits COMBINATION BASED ON FLUVALINATE AND THIOMETON, USEFUL FOR COMBATING INSECTS
JPH0618766B2 (en) * 1986-12-09 1994-03-16 北興化学工業株式会社 Acaricide composition
WO1988006842A1 (en) * 1987-03-13 1988-09-22 Sumitomo Chemical Company, Limited Stable solid pesticidal preparation
HU205839B (en) * 1987-11-18 1992-07-28 Chinoin Gyogyszer Es Vegyeszet Synergetic artropodicide composition containining pirethroides and phosphate-esters as active components

Also Published As

Publication number Publication date
FR2652716B1 (en) 1993-01-22
IT1247726B (en) 1994-12-30
US5120721A (en) 1992-06-09
CN1033356C (en) 1996-11-27
JP2813993B2 (en) 1998-10-22
ES2032255B1 (en) 1994-01-16
CN1050665A (en) 1991-04-17
IT9048341A1 (en) 1992-04-04
ES2032255A1 (en) 1993-01-16
IT9048341A0 (en) 1990-10-04
FR2652716A1 (en) 1991-04-12
KR0168434B1 (en) 1999-01-15
KR910007423A (en) 1991-05-30

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